HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 13300848, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13300847 | HCID 13300847 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 13300848 | HCID 13300848 | — |
Reaction Steps
3-(4(p-trifluoromethylphenoxy)phenyl)-4-phenylbutyric acid (23 g) was refluxed in benzene with thionyl chloride (46 ml) for one hour. The solution was then evaporated to dryness and the residue dissolved in benzene (23 ml). A solution of stannic chloride (23 g) in benzene (46 ml) was added at 0° with stirring. The solution was allowed to stir at 0° for 0.5 hr. Ice; water, diethylether and dilute HCl were then added sequentially. The ether extracts were further washed with aqueous potassium hydroxide and evaporated to give 3-(4-(p-trifluoromethylphenoxy)phenyl)tetralone m.p. 136°-137° (ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04520007 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-ddca9abd250f4496b7dfd262b8fdeefe |
| Source note | uspto-grants-1985_05 |